Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/A/G | Ancestral: T | Ambiguity code: D | MAF: 0.26 (T)

Chromosome 1:225423464 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60010985

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 12 transcripts and has 3696 sample genotypes.

Variant displays